Manufacturing Technician at Advanced Resources

Description

Responsible for cleaning, sanitizing, operating and maintaining process equipment used during the manufacture of sterile nasal spray drug products and for completing the associated documentation. Duties also include cleaning, organizing and monitoring manufacturing clean rooms. 

·       Follow Production Batch Records (PBRs) to operate, monitor and control equipment and process parameters during manufacture.

·       Follow SOPs to clean, sanitize and prepare process equipment for manufacturing. Follow SOPs to clean and sanitize rooms as required.

·       Complete PBRs, Logbooks, Forms and other documentation. Assist in compilation and review of lot records prior to submitting to QA.

·       Write and revise SOPs and Forms to accurately reflect the current procedures.

·       Maintain assigned manufacturing area neat, clean and well stocked with supplies

·       Assist with the training of other manufacturing team members.

·       Coordinate manufacturing, calibration and maintenance activities with other departments.

·       Assist with the writing, execution, and review of validation protocols for manufacturing/support equipment.

·       Independently champion manufacturing or facility related improvement projects.

·       Participate in the performance routine preventive maintenance on facilities and equipment.

·       Help identify continuous improvement and cost savings opportunities.

·       Adhere to cGMPs, SOPs, and Safety policies.

·       Other duties as assigned.

·       Excellent organizational skills and attention to detail.

·       Strong interpersonal and communication skills.

·       Motivated to perform work while maintaining a focus on the long-term learning and self-improvement.

·       Must be flexible, adaptable, self-motivated and able to work well independently and across teams and partners.

·       Ability to work in a lean, action oriented organization and demonstrate a strong work ethic

·       Good written communication skills to read and write SOPs and complete documents.

·       Pharmaceutical experience is preferred.

·       Experienced with Microsoft Word and Excel.

Qualifications

·       BS in a scientific discipline or equivalent experience.

·       0 - 5 years of applicable experience working in a pharmaceutical manufacturing environment.

·       Experience with sterilization processes or aseptic technique preferred.

·       Good written communication skills to write SOPs and other cGMP documents.

·       Qualified to work with controlled substances.

·       Strong interpersonal skills and the ability to work well in a team environment.

·       Qualified to work with controlled substances.